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Abstracts - Association for Chemoreception Sciences

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were phenotyped <strong>for</strong> detection thresholds <strong>for</strong> sweet (sucrose),<br />

savory (monosodium glutamate), and salty (NaCl) taste using<br />

age-appropriate psychophysical testings, dietary habits, blood<br />

pressure and obesity. Preliminary analyses revealed that the<br />

detection threshold <strong>for</strong> sucrose, salt, and MSG are similar to<br />

that previously reported in adults and there were no differences<br />

observed between normal weight children and obese children in<br />

the detection thresholds <strong>for</strong> any of these basic tastes. In normalweight,<br />

but not obese children, salt detection thresholds were<br />

positively correlated with systolic blood pressure. As a group, the<br />

greater the waist circumference, the lower the sucrose detection<br />

threshold (the more sensitive the child was to sucrose) (p=0.02).<br />

No such relationships existed <strong>for</strong> salt or MSG in children.<br />

Whether the lower detection thresholds <strong>for</strong> sucrose are associated<br />

with stronger rein<strong>for</strong>cing value of sweet foods, as has been<br />

observed in adults, and understanding the link between salt taste<br />

thresholds and blood pressure, are important areas <strong>for</strong> future<br />

research. Acknowledgements: This project was funded by an<br />

investigator-initiated grant from Ajinomoto, Inc.<br />

#P235 POSTER SESSION V:<br />

HUMAN TASTE PSYCHOPHYSICS;<br />

OLFACTION RECEPTORS; TASTE DEVELOPMENT<br />

Statistical Analysis of Factors Previously Described as<br />

Significant in the Ability to Taste Propylthiouracil Yields<br />

Roles <strong>for</strong> Age, Sex and Tas2r38 Haplotype, but not<br />

Fungi<strong>for</strong>m Papillae Density<br />

Nicole L. Garneau, Tiffany Derr<br />

Denver Museum of Nature & Science Denver, CO, USA<br />

The Genetics of Taste research study at the Denver Museum<br />

of Nature & Science is in a unique position to collect samples<br />

from a diverse population across a wide age range. Using this<br />

large population sample we set out to establish the scientific<br />

credibility of our community-based laboratory by replicating four<br />

previously reported statistically significant factors in the ability<br />

to taste propylthiouracil; 1)Age, 2)Sex, 3)Tas2r38 haplotype, and<br />

4)Fungi<strong>for</strong>m papillae density. Using regression analysis and the<br />

Student T-test we can replicate the role of age and sex in taste<br />

score (gLMS following a propylthiouracil taste test). Similarly,<br />

the presence of at least one dominant allele <strong>for</strong> the Tas2r38 gene<br />

is a significant predictor of taste. Finally, in order to decrease<br />

subjectivity, we developed a dichotomous key <strong>for</strong> objective<br />

analysis of fungi<strong>for</strong>m papillae density. Using this method we did<br />

not find that increased papillae density correlates to an increased<br />

propylthiouracil taste score. In conclusion, the ability to replicate<br />

the significance of age, sex and Tas2r38 haplotype, as well as the<br />

development of objective methodology <strong>for</strong> papillae analysis, all<br />

demonstrate the ability <strong>for</strong> citizen-scientists in a communitybased<br />

laboratory to collect, prepare and analyze data that can<br />

contribute to the field of chemoreception. In addition, we submit<br />

that using standardized methodology <strong>for</strong> fungi<strong>for</strong>m papillae<br />

density allows <strong>for</strong> a more objective analysis of morphological<br />

data. Using this methodology we find no relationship between<br />

fungi<strong>for</strong>m papillae density and propylthiouracil score in our<br />

data set. This data contradicts previously published studies and<br />

suggests that fungi<strong>for</strong>m papillae density may not be as reliable<br />

a metric <strong>for</strong> classifying taster status as previously thought.<br />

Acknowledgements: This work was supported by volunteer<br />

citizen-scientists at the Denver Museum of Nature & Science,<br />

and through support from 2008-2012 from R25 RR025066 NIH<br />

NCRR SEPA.<br />

#P236 POSTER SESSION V:<br />

HUMAN TASTE PSYCHOPHYSICS;<br />

OLFACTION RECEPTORS; TASTE DEVELOPMENT<br />

The effects of temperature on sequential and mixture<br />

interactions between sucrose and saccharin<br />

Barry G Green 1,2 , Danielle Nachtigal 1<br />

1<br />

The John B. Pierce Laboratory New Haven, CT, USA,<br />

2<br />

Yale University School of Medicine New Haven, CT, USA<br />

The sweet taste of sucrose and saccharin has been shown to<br />

depend on stimulation of the T1R2-T1R3 receptor, but it is<br />

also clear that these two stimuli interact with the receptor in<br />

different ways. Most recently it was found that self-adaptation is<br />

temperature-dependent <strong>for</strong> sucrose but not <strong>for</strong> saccharin (Green<br />

& Nachtigal, 2012), and a previous study showed that high<br />

concentrations of saccharin can block the sweetness of sucrose<br />

(and of itself) and evoke a sweet water taste (Galindo-Cusperino<br />

et al, 2006). The aim of the present study was to determine if<br />

temperature modulates the ability of sucrose to cross-adapt<br />

saccharin and/or of saccharin to block the sweetness of sucrose<br />

and produce a sweet water taste. Subjects rated the sweetness<br />

and bitterness of 0.42 M sucrose, 3.2 mM saccharin, 100 mM<br />

saccharin, or binary mixtures of sucrose and the 2 concentrations<br />

of saccharin, with and without pre-exposure to themselves or<br />

each of the other stimuli. The variables of interest were the<br />

duration of pre-exposure (3 or 10 s) and solution temperature<br />

(37° or 21°C). The stimuli were sampled by dipping the tongue<br />

tip into the solutions, and intensity ratings were made on the<br />

gLMS be<strong>for</strong>e the tongue was retracted back into the mouth.<br />

The results confirmed the previous findings and showed that (1)<br />

the magnitude of sweet water taste (after exposure to 100 mM<br />

saccharin) is temperature-dependent, and (2) surprisingly, preexposure<br />

to sucrose <strong>for</strong> 3 or 10 sec appeared to counteract the<br />

ability of 100 mM saccharin to block sweetness, independent of<br />

temperature. These results support the hypothesis that sucrose<br />

and saccharin bind to at least 2 different sites on the T1R2-T1R3<br />

receptor and raise new questions about the factors that can<br />

affect excitatory and inhibitory interactions between these sites.<br />

Acknowledgements: Supported in part by NIH grant DC005002<br />

POSTER PRESENTATIONS<br />

<strong>Abstracts</strong> are printed as submitted by the author(s).<br />

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